Beijing Bywave Sensing Medical Technology Co., Ltd.
ChinaFDA applicant, unverified FDA FEI 3018784828
- Devices
- 1
- Registrations
- FDA
- FDA recalls
- 0
At a glance
Market reach
- United States
- FDA FEI
Catalogue
DeviceDevice · Authorizations Verified Status Regime Registry Class
LiPPS Analyzer, LiPPS Wire Pressure Guide Wire Ref K201720
Regimes: 510(k) Registry: 510(k)
Company details
- FDA FEI number
- 3018784828
- Address
- Room 301, 1st to 3rd Floor, Building 33, Yard 6, Hengye 7th Street, Tongzhou District Beijing, P. R. China, BEIJING
Frequently asked questions
How many devices does Beijing Bywave Sensing Medical Technology Co., Ltd. have in the registry?
The registry currently lists 1 device for Beijing Bywave Sensing Medical Technology Co., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Beijing Bywave Sensing Medical Technology Co., Ltd.'s devices?
Among its 1 most recently registered device, Beijing Bywave Sensing Medical Technology Co., Ltd. has devices listed in FDA 510(k) (1 device).
What risk classes do Beijing Bywave Sensing Medical Technology Co., Ltd.'s devices fall under?
Among its 1 most recently registered device, the classes recorded for Beijing Bywave Sensing Medical Technology Co., Ltd.'s devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from Beijing Bywave Sensing Medical Technology Co., Ltd. in the registry?
The most recently registered devices listed for Beijing Bywave Sensing Medical Technology Co., Ltd. include LiPPS Analyzer, LiPPS Wire Pressure Guide Wire.